SIRO Clinpharm is one of the leading Global Clinical Research Organizations (CROs), offering full scope services conducting clinical trials in the Pharmaceutical, Biotechnology and Medical Devices sectors in compliance with International Standards. We are headquartered in India having global presence in USA, Israel and in Europe at Germany, Czech Republic, Greece, Estonia, Romania, Spain and France.
WALK IN INTERVIEW is open for the following functions:
1. Narrative Reviewers: Minimal 4-5 yrs of experience in Regulatory Medical Writing, primarily in clinical/ patient narratives.
2. Regulatory Medical Writers & Reviewers: 3-6 yrs of experience in authoring, reviewing/project managing CSRs, IBs, protocols, summary documents across all TAs.
3. DSRM (Drug Safety & Risk Management) Writers & Reviewers: 2-6 yrs of experience in authoring & reviewing of aggregate reports (DSURs, PSURs/ PBRERs, PADERs). Experience in RMPs would be an added advantage.
4. HEOR Analyst: 2-4 yrs of experience in translating health outcomes research into effective message development and communications.
5.Sr. Publication Writer: 4–5 yrs of exp in authoring & reviewing of publication documents
WALK IN DETAILS
Date: 25th and 26th November, 2016
Time: 10.00 am - 4.00 pm
Venue : Trident, Hyderabad HITEC City Near Cyber Towers, Madhapur Hyderabad - 500081, India
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